FDA Inspection 1030175 — Evotronics Inc

Evotronics Inc — FEI 3012514261

The FDA completed an inspection of Evotronics Inc on Oct 23, 2017 in Brooklyn Park, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 23, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Park, MN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
405921 CFR 820.22Quality Audits - defined intervals